Furosemide
- Product NDC
- 50090-6219
- 11-digit product format
- 500906219
- Labeler code
- 50090
- Product ID
- 50090-6219_53f4477e-13d8-402e-aa02-8a1e9addd00a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6219-0 | 50090621900 | 30 TABLET in 1 BOTTLE (50090-6219-0) | 30 tablet | 2022-11-10 | No | No | Historical |
| 50090-6219-1 | 50090621901 | 100 TABLET in 1 BOTTLE (50090-6219-1) | 100 tablet | 2022-11-10 | No | No | Historical |
| 50090-6219-7 | 50090621907 | 200 TABLET in 1 BOTTLE (50090-6219-7) | 200 tablet | 2022-11-10 | No | No | Historical |
| 50090-6219-8 | 50090621908 | 90 TABLET in 1 BOTTLE (50090-6219-8) | 90 tablet | 2022-11-10 | No | No | Historical |